A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9649980



Internal ID13593089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122804279..122804298hg38UCSC Ensembl
Innerchr10:122804275..122804302hg38UCSC Ensembl
Outerchr10:122804256..122804321hg38UCSC Ensembl
chr10:124563795..124563814hg19UCSC Ensembl
Innerchr10:124563791..124563818hg19UCSC Ensembl
Outerchr10:124563772..124563837hg19UCSC Ensembl
chr10:124553785..124553804hg18UCSC Ensembl
Innerchr10:124553808..124553781hg18UCSC Ensembl
Outerchr10:124553762..124553827hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3397858
Supporting Variants
SamplesNA12812
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9649980
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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